FunciSNP: an R/bioconductor tool integrating functional non-coding data sets with genetic association studies to identify candidate regulatory SNPs
about
Genome-wide association studies identify four ER negative-specific breast cancer risk lociMaking sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genomeCandidate gene association studies: a comprehensive guide to useful in silico toolsEnhancer scanning to locate regulatory regions in genomic lociA meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locusA meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.LocusExplorer: a user-friendly tool for integrated visualization of human genetic association data and biological annotations.On the identification of potential regulatory variants within genome wide association candidate SNP sets.Identification of putative pathogenic SNPs implied in schizophrenia-associated miRNAs.Functional annotation of colon cancer risk SNPs.FunSeq2: a framework for prioritizing noncoding regulatory variants in cancerGenetic variation in mitotic regulatory pathway genes is associated with breast tumor gradeRole of non-coding sequence variants in cancer.Enhancer variants: evaluating functions in common disease.Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.Comprehensive functional annotation of seventy-one breast cancer risk Loci.Enlight: web-based integration of GWAS results with biological annotationsInherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer.A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements.Obesity-related known and candidate SNP markers can significantly change affinity of TATA-binding protein for human gene promoters.Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in LungIntegration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions.Candidate SNP markers of aggressiveness-related complications and comorbidities of genetic diseases are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters.GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathwaymotifbreakR: an R/Bioconductor package for predicting variant effects at transcription factor binding sitesGLANET: Genomic Loci ANnotation and Enrichment Tool.A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.Genome-wide association study identifies two new susceptibility loci for colorectal cancer at 5q23.3 and 17q12 in Han Chinese.Chromatin interactions and candidate genes at ten prostate cancer risk loci.Candidate SNP Markers of Gender-Biased Autoimmune Complications of Monogenic Diseases Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene PromotersEnrichment of risk SNPs in regulatory regions implicate diverse tissues in Parkinson's disease etiology.Candidate SNP Markers of Chronopathologies Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene Promoters.Lessons from postgenome-wide association studies: functional analysis of cancer predisposition lociThe importance of detailed epigenomic profiling of different cell types within organs.Comprehensive functional annotation of 77 prostate cancer risk loci.Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1.Functional annotation of sixty-five type-2 diabetes risk SNPs and its application in risk predictionReducing GWAS Complexity.
P2860
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P2860
FunciSNP: an R/bioconductor tool integrating functional non-coding data sets with genetic association studies to identify candidate regulatory SNPs
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@ast
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@en
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@nl
type
label
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@ast
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@en
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@nl
prefLabel
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@ast
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@en
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@nl
P2860
P50
P356
P1476
FunciSNP: an R/bioconductor to ...... tify candidate regulatory SNPs
@en
P2093
Gerhard A Coetzee
Suhn K Rhie
P2860
P356
10.1093/NAR/GKS542
P407
P577
2012-06-08T00:00:00Z